Prognostic Significance of Urinary Biomarkers in Patients Hospitalized With COVID-19.

Acute kidney injury (AKI) COVID-19 prognosis chronic kidney disease (CKD) coronavirus disease 2019 (COVID-19) death dialysis epidermal growth factor (EGF) inflammatory marker kidney injury molecule 1 (KIM-1) monocyte chemoattractant protein 1 (MCP-1) neutrophil gelatinase-associated lipocalin (NGAL) severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) subclinical AKI tubular injury urinalysis urinary biomarkers urine microscopy

Journal

American journal of kidney diseases : the official journal of the National Kidney Foundation
ISSN: 1523-6838
Titre abrégé: Am J Kidney Dis
Pays: United States
ID NLM: 8110075

Informations de publication

Date de publication:
02 2022
Historique:
received: 30 04 2021
accepted: 01 09 2021
pubmed: 29 10 2021
medline: 29 1 2022
entrez: 28 10 2021
Statut: ppublish

Résumé

Acute kidney injury (AKI) is common in patients with coronavirus disease 2019 (COVID-19) and associated with poor outcomes. Urinary biomarkers have been associated with adverse kidney outcomes in other settings and may provide additional prognostic information in patients with COVID-19. We investigated the association between urinary biomarkers and adverse kidney outcomes among patients hospitalized with COVID-19. Prospective cohort study. Patients hospitalized with COVID-19 (n=153) at 2 academic medical centers between April and June 2020. 19 urinary biomarkers of injury, inflammation, and repair. Composite of KDIGO (Kidney Disease: Improving Global Outcomes) stage 3 AKI, requirement for dialysis, or death within 60 days of hospital admission. We also compared various kidney biomarker levels in the setting of COVID-19 versus other common AKI settings. Time-varying Cox proportional hazards regression to associate biomarker level with composite outcome. Out of 153 patients, 24 (15.7%) experienced the primary outcome. Twofold higher levels of neutrophil gelatinase-associated lipocalin (NGAL) (HR, 1.34 [95% CI, 1.14-1.57]), monocyte chemoattractant protein (MCP-1) (HR, 1.42 [95% CI, 1.09-1.84]), and kidney injury molecule 1 (KIM-1) (HR, 2.03 [95% CI, 1.38-2.99]) were associated with highest risk of sustaining primary composite outcome. Higher epidermal growth factor (EGF) levels were associated with a lower risk of the primary outcome (HR, 0.61 [95% CI, 0.47-0.79]). Individual biomarkers provided moderate discrimination and biomarker combinations improved discrimination for the primary outcome. The degree of kidney injury by biomarker level in COVID-19 was comparable to other settings of clinical AKI. There was evidence of subclinical AKI in COVID-19 patients based on elevated injury biomarker level in patients without clinical AKI defined by serum creatinine. Small sample size with low number of composite outcome events. Urinary biomarkers are associated with adverse kidney outcomes in patients hospitalized with COVID-19 and may provide valuable information to monitor kidney disease progression and recovery.

Identifiants

pubmed: 34710516
pii: S0272-6386(21)00920-3
doi: 10.1053/j.ajkd.2021.09.008
pmc: PMC8542781
pii:
doi:

Substances chimiques

Biomarkers 0
Lipocalin-2 0
Creatinine AYI8EX34EU

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

257-267.e1

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK106962
Pays : United States
Organisme : NIH HHS
ID : S10 OD026880
Pays : United States
Organisme : NIH HHS
ID : S10 OD030463
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK128538
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK117065
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK093770
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK079310
Pays : United States

Investigateurs

Albert Ko (A)
Akiko Iwasaki (A)
Shelli Farhadian (S)
Allison Nelson (A)
Arnau Casanovas-Massana (A)
Elizabeth B White (EB)
Wade Schulz (W)
Andreas Coppi (A)
Patrick Young (P)
Angela Nunez (A)
Denise Shepard (D)
Irene Matos (I)
Yvette Strong (Y)
Kelly Anastasio (K)
Kristina Brower (K)
Maxine Kuang (M)
Michael Chiorazzi (M)
Santos Bermejo (S)
Pavithra Vijayakumar (P)
Bertie Geng (B)
John Fournier (J)
Maksym Minasyan (M)
M Catherine Muenker (MC)
Adam J Moore (AJ)
Girish Nadkarni (G)

Informations de copyright

Copyright © 2021 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Auteurs

Steven Menez (S)

Division of Nephrology, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland.

Dennis G Moledina (DG)

Section of Nephrology and Clinical and Translational Research Accelerator, Department of Internal Medicine, School of Medicine, Yale University, New Haven, Connecticut.

Heather Thiessen-Philbrook (H)

Division of Nephrology, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland.

F Perry Wilson (FP)

Section of Nephrology and Clinical and Translational Research Accelerator, Department of Internal Medicine, School of Medicine, Yale University, New Haven, Connecticut.

Wassim Obeid (W)

Division of Nephrology, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland.

Michael Simonov (M)

Section of Nephrology and Clinical and Translational Research Accelerator, Department of Internal Medicine, School of Medicine, Yale University, New Haven, Connecticut.

Yu Yamamoto (Y)

Section of Nephrology and Clinical and Translational Research Accelerator, Department of Internal Medicine, School of Medicine, Yale University, New Haven, Connecticut.

Celia P Corona-Villalobos (CP)

Division of Nephrology, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland.

Crystal Chang (C)

Division of Nephrology, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland.

Brian T Garibaldi (BT)

Division of Pulmonary and Critical Care, Department of Medicine, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, 3Division of Medical Microbiology, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland.

William Clarke (W)

Division of Clinical Chemistry, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland.

Shelli Farhadian (S)

Section of Infectious Disease, Department of Internal Medicine, School of Medicine, Yale University, New Haven, Connecticut.

Charles Dela Cruz (C)

Section of Pulmonary and Critical Care Medicine, Department of Internal Medicine, School of Medicine, Yale University, New Haven, Connecticut.

Steven G Coca (SG)

Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Chirag R Parikh (CR)

Division of Nephrology, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland. Electronic address: chirag.parikh@jhmi.edu.

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